IP Library Granted Patent US 7,138,035
Granted Patent B2
US 7,138,035 · App. 09/851,069 · Granted Nov 21, 2006

Process for the selective modification of carbohydrates by peroxidase catalyzed oxidation

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Quick Facts
Patent No.
US 7,138,035
App. No.
09/851,069
Granted
Nov 21, 2006
Kind
B2
Abstract

The present invention relates to an environmentally friendly process for the selective oxidation of carbohydrates. The process comprises the addition of a hydroperoxide, including hydrogen peroxide, to a carbohydrate having primary alcohol groups, particularly including polysaccharides, wherein said carbohydrate is contact with a nitroxyl radical mediator and the process is catalyzed by a peroxidase enzyme in the presence of halide ions.

Claims (19)

1. A method of oxidizing carbohydrates having primary alcohol groups, the method comprising the steps of:

placing a nitroxyl radical mediator, halide and peroxidase enzyme in solution

with the carbohydrates, and

adding a hydroperoxide to the solution containing carbohydrates thereby oxidizing the carbohydrates.

2. The method of claim 1 wherein the hydroperoxide is hydrogen peroxide.

3. The method of claim 1 wherein the carbohydrate is a polysaccharide.

4. The method of claim 3 wherein the polysaccharide is selected from the group consisting of starch and cellulose pulp.

5. The method of claim 1 wherein the nitroxyl radical mediator is a di-tertiary alkyl nitroxyl radical has a formula selected from the group consisting of:

wherein A represents a chain of preferably two or three atoms, in particular carbon atoms or a combination of one or two carbon atoms with an oxygen or nitrogen atom, and the R groups represent the same or different alkyl groups.

6. The method of claim 5 wherein the nitroxyl radical mediator has the formula:

where Y is H, OH, O—C(O)—CH, or NH—C(O)—CH 3 .

7. The method of claim 2 wherein the peroxidase enzyme is derived from an animal source.

8. The method of claim 2 wherein the peroxidase enzyme is selected from the group consisting of lactoperoxidase (“LPO”), myeloperoxidase (“MPO”), eosinophil peroxidase (“EPO”), thyroid peroxidase (“TPO”), ovoperoxidase, salivary peroxidase, and vanadium haloperoxidase.

9. The method of claim 1 wherein the halide ion is bromide.

10. The method of claim 1 wherein the peroxidase enzyme is LPO; the temperature of the reaction is kept between about 10° C to about 70° C the pH is between about 3.0 to about 9.0; and the nitroxyl radical mediator is present in an amount of between about 0.01 to about 50 wt % by weight of the carbohydrate.

11. The method of claim 10 wherein the temperature of the reaction is kept between about 20° to about 50° ; the pH is between about 4.5 to about 6.5; and the nitroxyl radical mediator is present in an amount of between about 0.1 to about 20 wt % by weight of the carbohydrate.

12. The method according to claim 1 wherein the hydroperoxide oxidizes the halide to its corresponding hypohalite by catalytic action of the peroxidase enzyme, and

wherein the hypohalite oxidizes the nitroxyl radical mediator to its corresponding nitrosonium ion.

13. The method according to claim 12 wherein the nitrosonium ion oxidizes primary alcohols of the carbohydrates to aldehydes.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 12, 2008
From: NATIONAL STARCH AND CHEMICAL INVESTMENT HOLDING CORPORATION
To: BRUNOB II B.V.
Reel/Frame 021096/0293 →